A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv938033



Internal ID16231989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:12743679..12776013hg38UCSC Ensembl
Innerchr20:12724326..12756660hg19UCSC Ensembl
Innerchr20:12672326..12704660hg18UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg3832335
hg1932335
hg1832335
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv585433
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv938033
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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